A comprehensive evaluation of PCR primers to amplify the nifH gene of nitrogenase.

The nifH gene is the most widely sequenced marker gene used to identify nitrogen-fixing Bacteria and Archaea. Numerous PCR primers have been designed to amplify nifH, but a comprehensive evaluation of nifH PCR primers has not been performed. We performed an in silico analysis of the specificity and...

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Main Authors: John Christian Gaby, Daniel H Buckley
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3405036?pdf=render
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spelling doaj-fc64ab1dbdc24e018b0dd7434bce15612020-11-24T21:44:51ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0177e4214910.1371/journal.pone.0042149A comprehensive evaluation of PCR primers to amplify the nifH gene of nitrogenase.John Christian GabyDaniel H BuckleyThe nifH gene is the most widely sequenced marker gene used to identify nitrogen-fixing Bacteria and Archaea. Numerous PCR primers have been designed to amplify nifH, but a comprehensive evaluation of nifH PCR primers has not been performed. We performed an in silico analysis of the specificity and coverage of 51 universal and 35 group-specific nifH primers by using an aligned database of 23,847 nifH sequences. We found that there are 15 universal nifH primers that target 90% or more of nitrogen fixers, but that there are also 23 nifH primers that target less than 50% of nifH sequences. The nifH primers we evaluated vary in their phylogenetic bias and their ability to recover sequences from commonly sampled environments. In addition, many of these primers will amplify genes that do not mediate nitrogen fixation, and thus it would be advisable for researchers to screen their sequencing results for the presence of non-target genes before analysis. Universal primers that performed well in silico were tested empirically with soil samples and with genomic DNA from a phylogenetically diverse set of nitrogen-fixing strains. This analysis will be of great utility to those engaged in molecular analysis of nifH genes from isolates and environmental samples.http://europepmc.org/articles/PMC3405036?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author John Christian Gaby
Daniel H Buckley
spellingShingle John Christian Gaby
Daniel H Buckley
A comprehensive evaluation of PCR primers to amplify the nifH gene of nitrogenase.
PLoS ONE
author_facet John Christian Gaby
Daniel H Buckley
author_sort John Christian Gaby
title A comprehensive evaluation of PCR primers to amplify the nifH gene of nitrogenase.
title_short A comprehensive evaluation of PCR primers to amplify the nifH gene of nitrogenase.
title_full A comprehensive evaluation of PCR primers to amplify the nifH gene of nitrogenase.
title_fullStr A comprehensive evaluation of PCR primers to amplify the nifH gene of nitrogenase.
title_full_unstemmed A comprehensive evaluation of PCR primers to amplify the nifH gene of nitrogenase.
title_sort comprehensive evaluation of pcr primers to amplify the nifh gene of nitrogenase.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description The nifH gene is the most widely sequenced marker gene used to identify nitrogen-fixing Bacteria and Archaea. Numerous PCR primers have been designed to amplify nifH, but a comprehensive evaluation of nifH PCR primers has not been performed. We performed an in silico analysis of the specificity and coverage of 51 universal and 35 group-specific nifH primers by using an aligned database of 23,847 nifH sequences. We found that there are 15 universal nifH primers that target 90% or more of nitrogen fixers, but that there are also 23 nifH primers that target less than 50% of nifH sequences. The nifH primers we evaluated vary in their phylogenetic bias and their ability to recover sequences from commonly sampled environments. In addition, many of these primers will amplify genes that do not mediate nitrogen fixation, and thus it would be advisable for researchers to screen their sequencing results for the presence of non-target genes before analysis. Universal primers that performed well in silico were tested empirically with soil samples and with genomic DNA from a phylogenetically diverse set of nitrogen-fixing strains. This analysis will be of great utility to those engaged in molecular analysis of nifH genes from isolates and environmental samples.
url http://europepmc.org/articles/PMC3405036?pdf=render
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